Cloning and characterization of Hunk, a novel mammalian SNF1-related protein kinase

Genomics. 2000 Jan 1;63(1):46-59. doi: 10.1006/geno.1999.6078.

Abstract

We previously identified a novel protein kinase, Hunk, by means of a degenerate PCR screen designed to isolate kinases expressed in the murine mammary gland. We now describe the molecular cloning, chromosomal localization, and activity of this kinase and characterize its spatial and temporal pattern of expression in the mouse. We have isolated a 5.0-kb full-length cDNA clone that contains the 714-amino-acid open reading frame encoding Hunk. Analysis of this cDNA reveals that Hunk is most closely related to the SNF1 family of serine/threonine kinases and contains a newly described SNF1 homology domain. Accordingly, antisera specific for Hunk detect an 80-kDa polypeptide with associated phosphotransferase activity. Hunk is located on distal mouse chromosome 16 in a region of conserved synteny with human chromosome 21q22. During fetal development and in the adult mouse, Hunk mRNA expression is developmentally regulated and tissue-specific. Moreover, in situ hybridization analysis reveals that Hunk expression is restricted to subsets of cells within a variety of organs in the adult mouse. These findings suggest a role for Hunk in murine development.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Cell Line
  • Cloning, Molecular
  • Embryo, Mammalian / enzymology
  • Female
  • Gene Expression Regulation, Developmental
  • Humans
  • Immunoblotting
  • In Situ Hybridization
  • Mammary Glands, Animal / enzymology
  • Mice
  • Mice, Inbred Strains
  • Molecular Sequence Data
  • Organ Specificity
  • Polymerase Chain Reaction
  • Protein Serine-Threonine Kinases / genetics*
  • Protein Serine-Threonine Kinases / isolation & purification
  • Protein Serine-Threonine Kinases / metabolism
  • Sequence Alignment

Substances

  • SNF1-related protein kinases
  • Protein Serine-Threonine Kinases